Clinical implication of HLA class I expression in breast cancer

Background Human leukocyte antigen (HLA)-class I molecules on tumor cells have been regarded as crucial sites where cytotoxic T lymphocytes (CTL) can recognize tumor-specific antigens and are strongly associated with anti-tumor activity. However, the clinical impact of HLA class I expression in brea...

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Published inBMC cancer Vol. 11; no. 1; p. 454
Main Authors Kaneko, Koichi, Ishigami, Sumiya, Kijima, Yuko, Funasako, Yawara, Hirata, Munetsugu, Okumura, Hiroshi, Shinchi, Hiroyuki, Koriyama, Chihaya, Ueno, Shinichi, Yoshinaka, Heiji, Natsugoe, Shoji
Format Journal Article
LanguageEnglish
Published London BioMed Central 20.10.2011
BioMed Central Ltd
BMC
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ISSN1471-2407
1471-2407
DOI10.1186/1471-2407-11-454

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Summary:Background Human leukocyte antigen (HLA)-class I molecules on tumor cells have been regarded as crucial sites where cytotoxic T lymphocytes (CTL) can recognize tumor-specific antigens and are strongly associated with anti-tumor activity. However, the clinical impact of HLA class I expression in breast cancer has not been clarified. Methods A total of 212 breast cancer patients who received curative surgery from 1993 to 2003 were enrolled in the current study. HLA class I expression was examined immunohistochemically using an anti-HLA class I monoclonal antibody. The correlation between HLA class I positivity and clinical factors was analyzed. Results The downregulation of HLA class I expression in breast cancer was observed in 69 patients (32.5%). HLA class I downregulation was significantly associated with nodal involvement (p < 0.05), TNM stage (p < 0.05), lymphatic invasion (p < 0.01), and venous invasion (p < 0.05). Patients with preserved HLA class I had significantly better disease-free interval (DFI) than those with loss of HLA class I (p < 0.05). However, in multivariable analysis, HLA class I was not selected as one of the independent prognostic factors of disease-free interval. Conclusion The examination of HLA class I expression is useful for the prediction of tumor progression and recurrent risk of breast cancer via the antitumor immune system.
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ISSN:1471-2407
1471-2407
DOI:10.1186/1471-2407-11-454